Short QT syndrome type 1

MONDO:0012312

Any short QT syndrome in which the cause of the disease is a mutation in the KCNH2 gene.

Also known as: KCNH2 short QT syndrome, SQTS, short QT syndrome caused by mutation in KCNH2, short QT syndrome type 1, SQT1, short QT syndrome 1

32 clinical trials for this condition and its sub-types, 0 tagged with Short QT syndrome type 1 itself.

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